Details for New Drug Application (NDA): 075139
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The generic ingredient in IBUPROFEN is ibuprofen sodium. There are sixty-four drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the ibuprofen sodium profile page.
Pharmacology for NDA: 075139
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 075139
Suppliers and Packaging for NDA: 075139
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
IBUPROFEN | ibuprofen | TABLET;ORAL | 075139 | ANDA | Walgreen Company | 0363-0393 | 0363-0393-20 | 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0393-20) |
IBUPROFEN | ibuprofen | TABLET;ORAL | 075139 | ANDA | Walgreen Company | 0363-0438 | 0363-0438-99 | 1 BOTTLE in 1 CARTON (0363-0438-99) / 100 TABLET, FILM COATED in 1 BOTTLE |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
Approval Date: | Mar 1, 1999 | TE: | RLD: | No |
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